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2019 2
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Page 1
Genetic landscape in Russian patients with familial left ventricular noncompaction.
Meshkov AN, Myasnikov RP, Kiseleva AV, Kulikova OV, Sotnikova EA, Kudryavtseva MM, Zharikova AA, Koretskiy SN, Mershina EA, Ramensky VE, Zaicenoka M, Vyatkin YV, Kharlap MS, Nikityuk TG, Sinitsyn VE, Divashuk MG, Kutsenko VA, Basargina EN, Barskiy VI, Sdvigova NA, Skirko OP, Efimova IA, Pokrovskaya MS, Drapkina OM. Meshkov AN, et al. Among authors: mershina ea. Front Cardiovasc Med. 2023 May 24;10:1205787. doi: 10.3389/fcvm.2023.1205787. eCollection 2023. Front Cardiovasc Med. 2023. PMID: 37342443 Free PMC article.
A Splice Variant of the MYH7 Gene Is Causative in a Family with Isolated Left Ventricular Noncompaction Cardiomyopathy.
Myasnikov RP, Kulikova OV, Meshkov AN, Bukaeva AA, Kiseleva AV, Ershova AI, Petukhova AV, Divashuk MG, Zotova ED, Sotnikova EA, Abisheva AA, Muraveva AV, Koretskiy SN, Popov SV, Utkina MV, Snigir EA, Mitrofanov SI, Konureeva KD, Mershina EA, Sinitsyn VE, Yudin SM, Drapkina OM. Myasnikov RP, et al. Among authors: mershina ea. Genes (Basel). 2022 Sep 28;13(10):1750. doi: 10.3390/genes13101750. Genes (Basel). 2022. PMID: 36292635 Free PMC article.
Predictive Value of Cardiac MRI in Patients with Fabry Disease.
Tao E, Moiseev A, Mershina E, Bobkova I, Moiseev S. Tao E, et al. Among authors: mershina e. Radiology. 2020 Aug;296(2):E123. doi: 10.1148/radiol.2020200909. Epub 2020 May 12. Radiology. 2020. PMID: 32396044 No abstract available.
A Case of Severe Left-Ventricular Noncompaction Associated with Splicing Altering Variant in the FHOD3 Gene.
Myasnikov R, Bukaeva A, Kulikova O, Meshkov A, Kiseleva A, Ershova A, Petukhova A, Divashuk M, Zotova E, Sotnikova E, Kharlap M, Zharikova A, Vyatkin Y, Ramensky V, Abisheva A, Muraveva A, Koretskiy S, Kudryavtseva M, Popov S, Utkina M, Mershina E, Sinitsyn V, Kogan E, Blagova O, Drapkina O. Myasnikov R, et al. Among authors: mershina e. Genes (Basel). 2022 Feb 7;13(2):309. doi: 10.3390/genes13020309. Genes (Basel). 2022. PMID: 35205353 Free PMC article.
The Desmin (DES) Mutation p.A337P Is Associated with Left-Ventricular Non-Compaction Cardiomyopathy.
Kulikova O, Brodehl A, Kiseleva A, Myasnikov R, Meshkov A, Stanasiuk C, Gärtner A, Divashuk M, Sotnikova E, Koretskiy S, Kharlap M, Kozlova V, Mershina E, Pilus P, Sinitsyn V, Milting H, Boytsov S, Drapkina O. Kulikova O, et al. Among authors: mershina e. Genes (Basel). 2021 Jan 19;12(1):121. doi: 10.3390/genes12010121. Genes (Basel). 2021. PMID: 33478057 Free PMC article.
16 results